Characterization and transformation of TtMYB1 transcription factor from Tritipyrum to improve salt tolerance in wheat

Background Common wheat (Triticum aestivum L.) is a worldwide cereal crop, which is an integral part of the diets of many countries. In addition, the MYB gene of wheat plays a role in the response to salt stress. Results “Y1805” is a Tritipyrum variety that is relatively tolerant to salt. We used transcriptome analysis to show that the “Y1805” MYB gene was both highly expressed and sensitive to salt stress. Compared with control roots, the level of MYB expression during salt stress was higher, which rapidly decreased to control levels during the recovery process. MYB gene relative expression showed the highest levels in “Y1805” roots during salt stress, with the stems and then leaves being the next highest stressed tissues. The novel MYB gene (TtMYB1) was successfully cloned from “Y1805”. It showed a coding sequence length of 783 bp with 95.79% homology with Tel2E01G633100 from Thinopyrum elongatum. TtMYB1 and MYB from Th. elongatum were clustered in the same branch using phylogenetic analysis, which indicated high similarities. The TtMYB1 gene is located in the nucleus. The coleoptile method was employed when a TtMYB1 overexpression vector was used during transformation into “1718” (common wheat). Under high salt stress, TtMYB1 leaves of overexpression lines had decreased wilting, when compared with wild-type (WT) plants. During normal conditions, salt stress, and recovery, the lengths of the roots and the heights of seedlings from the overexpression lines were found to be significantly greater than roots and seedlings of WT plants. In addition, during high salt stress, the overexpression lines showed that proline and soluble sugar levels were higher than that of WT plants, but with lower malondialdehyde levels. Forty-three proteins that interacted with TtMYB1 were identified using the yeast two-hybrid assay. Protein-protein interaction analyses indicated that most were SANT domain-containing and Wd repeat region domain-containing proteins. Among these proteins, ribosomal proteins were the main node. Abiotic stress-related terms (such as “carbonate dehydratase activity”, “protein targeting peroxisomes”, and “glutathione peroxidase activity”) were enriched in GO analysis. In KEGG analysis, “carbohydrate metabolism”, “environmental information processing”, “genetic information processing”, “signaling and cell precursors”, and “energy metabolism” pathways were enriched. Conclusion The TtMYB1 gene might enhance salt tolerance by increasing proline and soluble sugar content and antioxidase activity in transgenic wheat. It therefore has the potential to enhance high salt tolerance in plants. Supplementary Information The online version contains supplementary material available at 10.1186/s12864-024-10051-5.


Introduction
Common wheat (Triticum aestivum L.) is a worldwide cereal crop, which is an integral part of the diets of many countries [1].Soil salinization is a common factor that reduces crop growth and yield in modern agriculture [2,3].To cope with saline-alkaline stress, plants have evolved sophisticated regulatory mechanisms, including those involved in signal recognition and transduction, transcriptional regulation, and responses to high salt stress [4,5].It is therefore crucial to identify important genes for breeding crops resistant to high salt conditions.
MYB transcription factors (TFs) are only found in eukaryotes, comprising a large and diverse family of plant TFs.The TFs are involved in many essential physiological and biochemical processes [6,7].MYB TFs from plants have an N-terminal domain and MYB domain of approximately 51-52 amino acids.The repeats of MYB are characterized by a hydrophobic core that contains a total of three conserved tryptophan residues [8].A conserved DNA-binding domain is shared in MYB proteins, which is comprised of 1 − 4 partially nonhomologous amino acid sequence repeats.When considering the adjacent repeats, the plant proteins of MYB in plants are divided into four distinct groups: MYB-related (MYBR, which contains one R1 or the R2-like repeat, only), R2R3-MYB (with two R2/3R similar repeats), 3R-MYB (with three R1/R2/R3-like repeats), and atypical MYB proteins (4R-MYB, with four R1/R2-like repeats; similar to CDC5) [9].
The salt stress response is at least partially controlled by the MYB family [10].During high salt stress of plants, R2R3-MYB TFs mainly respond by participating in the abscisic acid (ABA) signaling pathway, regulating the levels of reactive oxygen species (ROS), and improving osmotic stress resistance [11,12].When there is overexpression of Arabidopsis, it can result in decreases in the levels of ABA-dependent gene transcripts during stress from high salt conditions [13].When TaMYB86B is overexpressed, there is an increase of wheat to high salt tolerance.This process involves the regulation of ion homeostasis, maintainance in osmotic balance, and a decrease in ROS levels [14].In rice, it was confirmed that the R2R3-type MYB gene, OsMYB91, was involved in tolerance to stress from high salt and in plant growth [15].Overexpression of the SlMYB102 gene helps to accumulate a large number of ROS scavengers, slow the rate of ROS production, and thereby improve tomato tolerance to high salt stress [16].An increase in the expression of MdMYB108L has been shown to be involved in increases of photosynthesis capacity of hairy root tissues (leaves) during salt stress, and it has also been shown that when bound to the salt-tolerant MdNHX1 promoter, it results in positive transcription in apples, to increase high salt tolerance in transgenic plants [17].
It has been reported that there was a diverse range of MYB TF functions in different plant species [8,9].Salt and polyethylene glycol significantly induce the expression of GhMYB108-like in upland cotton [18].When AmMYB1 TF is constitutively expressed in transgenic tobacco plants in salt-tolerant Avicennia marina, it is more resistant to high salt stress [19].GhMYB36 is a gene that encodes a R2R3-type MYB protein in Gossypium hirsutum.It results in tolerance to drought and wilt resistance to Verticillium wilt in Arabidopsis and cotton [20].The maintainance of Fe homeostasis is important when Arabidopsis responds to stress from ammonia, which has been correlated with the expressions of MYB28 and MYB29 [21].ZmMYB31, an R2R3-MYB TF in maize, is an important positive regulator of cold and peroxide stress.It is involved in the regulation of expression of genes involved in stress due to chilling, to decrease the levels of ion extravasation, the content of ROS, and low temperature photoinhibition, to improve resistance to low temperature [22].Drought and cold induce expression of ApMYB77, and overexpression in Arabidopsis has been shown to enhance tolerance to freezing [23].MYB59 plays a role in the responses to stress and plant growth as a negative regulator of homeostasis and calcium signaling [24].AtMYB96 is also involved in pathogen resistance via a mechanism inducing salicylic acid biosynthesis in Arabidopsis.Although they improve abiotic stress tolerance and pathogen resistance, plant R2R3-MYB TFs are also involved in defensive responses to insects.In wheat, TaMYB19, TaMYB29, and TaMYB44 have roles as coregulators of phloem-based defenses against the English grain aphid [25].
In Triticeae, E genome species (e.g., halophile wheatgrass Thinopyrum elongatum) is an important gene pool involved in wheat genetic improvement.It has genetic variations in many important agronomic traits, such as salt tolerance, cold tolerance, and disease resistance [26].Tritipyrum displays salt tolerance and is derived from crosses of Triticum aestivum and Th.elongatum [27].In addition, gene families of the MYB gene have been found in many plant species, including common wheat, rice, maize, tomato, apple, and Arabidopsis [16,17,22,23,25].Nonetheless, the studies of the MYB gene from the salttolerant Tritipyrum have not been reported.In the current study, TtMYB1, an R2R3-type MYB gene, was cloned from Tritipyrum, to characterize its sequence, evolutionary relationships, patterns of expression, gene functions, and the interactions of proteins during high salt stress.The present study therefore revealed an increased understanding of the salt-tolerant mechanism of MYB genes, and provides the basis for the breeding of more salt-tolerant wheat varieties.

MYB gene screening by transcriptomic analysis
Transcriptome analysis was carried out on the roots of salt-tolerant Tritipyrum "Y1805" and salt-sensitive wheat "Chinese spring" ("CS") after 5 h salt stress and 1 h recovery to select important genes in the response to salt stress.The relative expression level [log 2 fold change (log 2 FC) = 6.82] of Tel2E01G633100 in Tritipyrum "Y1805" was significantly higher than in wheat "CS" under salt stress (Table 1).However, this gene showed no change in expression after recovery in "Y1805".Basic local alignment search tool (BLAST) analysis indicates that Tel2E01G633100 contained two SANT domains, therefore it might be an MYB protein.Tel2E01G633100 was annotated and assigned to the gibberellic acid mediated signaling pathway (GO:0009740) and gibberellin biosynthetic process (GO:0009686) by GO analysis.Gibberellin can promote the elongation and growth of roots to enhance its water absorption capacity.Therefore, "Y1805" specific Tel2E01G633100 might be an important gene involved in the salt stress response.

Expression patterns of the MYB gene in Y1805
To investigate the spatial and temporal expression pattern of MYB, we analyzed the expression levels of MYB in roots under salt stress and recovery conditions and in various tissues using quantitative real-time PCR (qPCR) analysis.The relative expression level of the MYB gene was the highest under salt stress in the roots of "Y1805", stems were the next highest, and then leaves (Fig. 1A).The expression level of the MYB gene in the roots was 1.76 and 13.06-fold higher than those of stems and leaves, respectively.In addition, the MYB expression level was significantly (7.22-fold) higher than the control under salt stress in the roots.However, it dropped rapidly after recovery (Fig. 1B).These results were consistent with the above transcriptome data, indicating that "Y1805"-specific MYB were expressed highly and sensitively in the roots under salt stress to adapt.
Table 1 Relative expression level (log 2 FC) of Tel2E01G633100 under salt stress and recovery conditions in two wheat varieties
In bioinformatics analysis, TtMYB1 encoded 259 amino acids (aa).The TtMYB1 protein contained ten serine, three threonine, and two tyrosine residues, which could be protein kinase phosphorylation sites (Fig. 3A).Hydropathy plots predicted that TtMYB1 was predominantly hydrophilic, indicating it might play a role in plant salt stress tolerance (Fig. 3B).The TtMYB1 protein had SANT conserved domains at 20-70 aa and 73-121 aa in a region located at the N-terminal (Fig. 3C), indicating that TtMYB1 belongs to the 2R3R-type MYB transcription factor, and the domains might participate in the formation of a homo/heterodimer and regulate of transcription, respectively.The phylogenetic tree of wheat MYB protein was constructed, and TtMYB1 and Tel2E01G633100 were grouped together (Fig. 3D).TtMYB1 and MYB from Th. elongatum were clustered in the same branch, which indicates they have high similarity.Therefore, we speculated that TtMYB1 of Tritipyrum might be similar to that of Th. elongatum in evolution and function.

Homology modeling and molecular simulation of the TtMYB1 protein
Based on the Modeler 9.22 model, the N and C-terminal regions of the TtMYB1 protein had an α-helix and some reverse parallel β-chains (Fig. 4A).The compatibility between the model and c6kksA is 81.8%, indicating that the model is of good quality.The root mean square deviation (RMSD) analysis of the TtMYB1 protein backbone reached a peak (1.5312 nm) at 1257 picoseconds (ps), and the RMSD curve reached equilibrium after 1250 ps with a fluctuation range of 0.80-1.53nm (Fig. 4B).The Ramachandran plot of the protein showed that the conformation was accurate.Because the model was accurate in over 90% of its most favorable regions, which are indicated in red [A, B, L], it could be considered that the protein model conformed to the rules of stereochemistry.The favorable region of the protein model in this study reached 92.6%, allowing for 7.4% of the amino acid residues in the residual region, and no residues in the disallowed region (Fig. 4C).These results indicate that the TtMYB1 protein structure was stable.

Subcellular localization of TtMYB1
To investigate the subcellular location of the TtMYB1 proteins, a fusion protein transiently expressing 1300-TtMYB1-green fluorescence protein (GFP) was produced in tobacco mesophyll cells.The fluorescence emitted by the fusion protein was in the nucleus, overlapping the blue 4′,6-diamidino-2-phenylindole (DAPI) signal (Fig. 5), which means that TtMYB1 is located in the

Coleoptile transformation in common wheat
To determine TtMYB1 function, TtMYB1 was transformed and overexpressed in common wheat.The coleoptile tips of common wheat were cut to expose the meristem and infected with Agrobacteria containing the TtMYB1 gene.Transgenic-positive plants were confirmed by multiplex PCR using TtMYB1-specific primers and housekeeping 18 S gene primers.The housekeeping primers amplified in all plant samples indicate that the DNA was of good quality (Fig. 6; Supplementary Fig. S2).Lanes 1, 5, 8, 10, and 12 show amplification with construct-specific primer sets, indicating these plants had incorporated the transgene.

Overexpression of TtMYB1 enhanced salt tolerance in wheat Effect of salt stress on plant growth
Under NaCl stress, the leaves of TtMYB1-overexpressing wheat lines showed less wilting compared to these of the wild-type (WT) plants (Fig. 7A-D).Additionally, the overexpression lines exhibited a higher height and longer roots than the WT plants (Fig. 7E-H), indicating that the TtMYB1 gene conferred wheat with salt tolerance.
Under normal, salt stress, and recovery conditions, the root length and seedling height of the overexpression lines were significantly greater than those of WT plants (Fig. 8).This data suggested that overexpression of TtMYB1 improved plant growth and salt stress had a greater inhibitory effect on the growth of the WT plants compared to the overexpression lines at the seedling stage.

Effects of salt stress on physiological indicators
Proline accumulation is a common response to various abiotic stresses.It acts as an osmoprotectant, helping to protect cell membranes and proteins under stress [28,29].Under normal growth conditions, the proline content of the overexpression lines was slightly higher than that of the WT plants (Fig. 9A).After salt stress, the proline content of both the WT plants and overexpression lines significantly increased.With the extension of salt stress, the proline content in the overexpression lines increased rapidly, reached a peak at the T2 stage, and was significantly higher than that of the WT plants.After recovery, the proline content of the overexpression lines quickly dropped to the control level.These results indicated that the overexpression lines could respond more sensitively to salt stress to adapt quickly.
Soluble sugars act as osmotic substances and molecular chaperones to protect the structural and protein integrity and enhance enzyme activity, thus improving the resistance to abiotic stress [30].Under normal, salt stress, and recovery conditions, the soluble sugar content of the overexpression line was significantly higher than that of the WT plant (Fig. 9B).
When plants are subjected to various abiotic stresses, the activity of ROS increases, followed by the production of membrane lipid peroxidation product MDA, which damages plant cells and can lead to cell death in severe cases [31,32].Compared with the WT plants, the overexpression lines showed a significant decrease in MDA content under salt stress (Fig. 9C).The MDA content of the WT plants rapidly increased with the extension of salt stress and reached a peak at the T2 stage, which was 1.54-fold that of the overexpression lines.The degree of increase in MDA content in the overexpression lines was significantly less than that of WT plants under salt stress.This might be attributed to salt tolerance in the lines overexpressing the TtMYB1 gene.

Interacting protein analysis of TtMYB1
A yeast two-hybrid (Y2H) experiment was used to explore the proteins that interacted with TtMYB1 to enable a better understanding of the regulatory mechanism.The detection of self-activation showed that the control strains could grow normally on SD/-Leu/-Trp (SD-LW) plates, and three random colonies of pGADT7 + pGBKT7-TtMYB1 transporters could grow on SD/-Ade/-His/-Leu/-Trp (SD-ALWH) plates (Fig. 10A).This indicated that the TtMYB1 protein was self-activating, and could not be used directly to screen the cDNA library.The TtMYB1 was truncated into two fragments (TtMYB1-1 and TtMYB1-2, Table S1) for further detection of self-activation.For TtMYB1-1, there were white plaques on the SD-LW plate and sterile plaques on the SD-ALWH plate, indicating that the TtMYB1-1 was a non-toxic and non-self-activating protein (Fig. 10B).Therefore, TtMYB1-1 was used to screen the library.
The library plasmid and the TtMYB1-1-pGBKT7 bait plasmid were co-transfected into Y2HGold yeast competent cells and spread on SD-LW, SD-ALWH plates, and SD-ALWH (x-α-gal) plates.The positive control and clones could grow normally on the SD-LW, SD-ALWH, and SD-ALWH (x-α-gal) plates.The negative control could grow normally on the SD-LW plate, but it could not grow on the SD-ALWH and SD-ALWH (x-α-gal) plates, because it did not activate histidine, adenine, and x-α-gal reporter genes.In total, 51 clones were positive.Rotational validation experiments further showed that all 51 proteins might interact with TtMYB1 (Fig. 10C).The sequencing data and statistical results of the TtMYB1-interacting proteins are shown in Table S2.Eight proteins (such as XM_044551351.1,XM_044583951.1,and XM_044597708.1)were repetitively identified according to the sequencing data and BLAST analysis.Therefore, 43 interacting proteins were obtained except repetitive proteins.
Protein-protein interaction (PPI) analysis indicated that PPI occurred in 11 proteins; most of these were SANT domain and Wd repeat region domain-containing proteins, and were enriched in the process of protein synthesis.Important biological processes were screened by GO analysis, most of these were related to abiotic stress responses, such as "carbonate dehydratase activity" (GO:0005770), "protein targeting peroxisomes" (GO:0006625), and "glutathione peroxidase activity" (GO:0004602) (Table 2).Among these proteins, ribosomal proteins were the main node, suggesting that they might play a crucial role in the response of TtMYB1 to salt stress (Fig. 11A).Through Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis, we found that 24 proteins could be annotated to known functional genes.Among them, seven proteins were enriched in "genetic information processing", five in "signaling and cell precursors", three in "carbohydrate metabolism", two in "energy metabolism", one in "environmental information processing", and one in "cellular process" (Fig. 11B).

TtMYB1 and TtHHO5 interaction identified by bimolecular fluorescence complementation (BiFC) assays
An interesting interacting transcription factor TtHHO5 from wheat was identified in plant cells by the BiFC assay.When TtMYB1-nYFP (the N-terminal fragment of yellow fluorescent protein (YFP) was transiently co-expressed with TtHHO5-cYFP (the C-terminal fragment of YFP) in Nicotiana benthamiana leaves, reconstituted YFP fluorescence was observed in the nuclei, indicating an interaction between TtMYB1 and TtHHO5.However, no yellow fluorescent signal was observed when TtMYB1-nYFP and cYFP or TtHHO5-cYFP and nYFP were coexpressed (Fig. 12).Meanwhile, the proteins TtMYB1 and TtHHO5 were co-localized in blue nuclei, which coincided with their regulatory function.

Discussion
Cloning and expression characteristics of the TtMYB1 gene MYB genes are closely associated with abiotic stress tolerance, such as salinity stress, drought stress, and high temperature [10].Most of the R2R3-MYB genes and a few MYBR and 3R-MYB genes are known to be involved in salt stress regulation.Overexpression of the wheat TaMYB73 gene in A. thaliana enhances salt tolerance of transgenic plants and up-regulates the expression of several genes such as AtCBF3, AtABF3, AtRD29A, and AtRD29B [33].Rice OsMYB91 is an R2R3-MYB gene that is involved in tolerance to salt stress and plant growth by enhancing the ability to scavenge ROS [15].In this study, a unique TtMYB1 gene, which was upregulated under salt stress, was cloned from salt-tolerant Tritipyrum "Y1805".Amino acid sequences indicate that TtMYB1 contains a 2R3R domain (Fig. 3).TtMYB1 is a hydrophilic protein that is rich in leucine and glycine.The model has a high number of residues (92.60%) within the favored regions of the Ramachandran plot, making it a reliable 3D protein structure.Phylogenetic analysis of MYB proteins from various species showed that TtMYB1 had a close genetic relationship with those of Th. elongatum, indicating that TtMYB1 should originate from the E genome of Th. elongatum.
Salt tolerance is attributed to the significantly induced expression of abiotic stress-response genes [34].MdMYB108L overexpression also increased the photosynthetic capacity of hairy root tissue (leaves) under salt stress.In addition, the MdMYB108L TF bound to the MdNHX1 promoter positively regulates the transcription  of the salt tolerance gene MdNHX1 in apples, improving the salt tolerance of transgenic plants [17].Here, the relative expression level of the TtMYB1gene was the highest in the roots of "Y1805" under salt stress, stems were the next highest, and then leaves (Fig. 1A).The root system was directly and seriously damaged under salt stress.The TtMYB1 expression level in the roots was significantly higher than that in the control under salt stress.However, it dropped rapidly to the control level after recovery (Fig. 1B).Therefore, TtMYB1 was expressed highly and sensitively in the roots to adapt to salt stress.

Interacting proteins of TtMYB1
The MYB protein family is a large, functionally diverse family that is widely involved in plant biotic and abiotic stress responses [10].It is related to various biological processes, such as the responses to adversity stress such as salt stress, drought, and low temperature [35][36][37].In GO analysis, MYB genes that are differentially expressed in rice were found to be involved in the regulation of plant biological processes, such as responses to abiotic stress, endogenous stimuli, environmental stimuli, and regulation of two-component signal transduction systems [38,39].Arabidopsis MYBs are related to "lipid and energy metabolism", "osmoprotection", "terpenoid and flavonoid metabolism", and "signal transduction" [40].In this experiment, TtMYB1 interacting proteins are enriched in "genetic information processing", "environmental information processing", "carbohydrate metabolism", "signaling and cellular process", and "energy metabolism" pathways, which is consistent with previous results [38,40,41].MYB7 participates in salt stress during seed germination through the negative regulation of the bZIP TF ABI5 [42].In addition to flavonoid biosynthesis and ROS scavenging, overexpression of MYB12 also upregulated the expression of genes involved in ABA and proline biosynthesis, thus conferring plants with salt tolerance [43].This experiment found new proteins that interacted with TtMYB1, such as the proteins related to vitamin D receptor proteins (XM_020340878.3 and XM_044495777.1).These proteins might contribute to salt tolerance in Tritipyrum "Y1805" (Table S2).In addition, PPI analysis showed that ribosomal proteins were the main node, suggesting that they might participate in the efficient reorganization of protein biosynthetic machinery [44], which could be attributed to the salt tolerance of the TtMYB1 gene.
The HHO TF family is a new subfamily of the G2-like family in the GARP superfamily [45].MYB4 had a strong regulatory influence on HHO5 under salt stress in wheat [46].Expression of HHO5 increases in the first 6-12 h of salt stress in Arabidopsis, and it is most highly expressed in vegetative tissues, predominantly roots [47].Here, TtMYB1 and TaHHO5 showed an interaction by the Y2H and BiFC assays.It was speculated that TtMYB1 might have a regulatory effect on TtHHO5 in enhancing salt tolerance of the overexpression lines.

Effect of TtMYB1 gene on salt tolerance of transgenic wheat
The expression of some MYB genes is induced or inhibited by abiotic stress, which can increase the salt tolerance of transgenic plants [48,49].Similarly, our transcriptome results indicated that salinity stress could rapidly improve TtMYB1 gene expression, suggesting that TtMYB1 might play a critical role in the salinity stress response.Therefore, we transformed TtMYB1 into common wheat "1718" to analyze its tolerance to salt stress.Our finding suggested that the TtMYB1 overexpression lines had less leaf withering and longer roots compared to the WT plants (Figs. 7 and 8).TtMYB1 was similar to Tel2E01G633100 according to their cDNA sequences, so it was speculated that they could have a similarity in function.Tel2E01G633100 was assigned to the gibberellic acid mediated signaling pathway (GO:0009740) and gibberellin biosynthetic process (GO:0009686) by GO analysis.Gibberellin can promote the elongation and growth of roots for better water uptake under salt stress, which might be part of the reason for longer roots in "Y1805".When plants are subjected to drought and salinity stresses, some physiological indices can react quickly to enable these plants to survive under extreme environmental conditions [48,50].Under high salt stress conditions, the ROS and MDA content in the transgenic FtMYB13 plants decreased, whereas proline content and photosynthetic efficiency increased, which improved their salt tolerance [31].Physiological indices related to osmotic stress caused by drought and salinity can be used as a fast and accurate method for assessing plant resistance to abiotic stress [50][51][52].Abiotic stress has been reported to cause lipid peroxidation, leading to MDA accumulation [50,53].Here, the MDA content was higher in WT plants than in TtMYB1 overexpression lines (Fig. 9C), which indicated that salt stress damaged WT plants more than the overexpression lines.Therefore, the TtMYB1 gene might contribute to the cell membrane integrity of plants in response to salinity stress.In response to salt stress, proline and soluble sugar participate in osmotic regulation and maintain the structural stability of cells [54].In this study, the overexpression lines accumulated more proline and soluble sugar compared with the WT plants under salt stress (Fig. 9A,  B), which reduced the water potential of root cells, increased the water absorption and retention capacity of roots, and finally improved their salt tolerance.Therefore, our results demonstrate that salt tolerance of the TtMYB1 overexpression lines was partially related to higher proline and soluble sugar content, and lower levels of MDA.

Conclusion
A novel TtMYB1 gene was selected from salt-tolerant Tritipyrum "Y1805" based on transcriptome data.The TtMYB1 gene had a coding sequence length of 783 bp and had 95.79% identity to Tel2E01G633100 from Th. elongatum.A phylogenetic tree showed that TtMYB1 and MYB from Th. elongatum were clustered on the same branch.The TtMYB1 gene was significantly upregulated in "Y1805" roots to adapt to salt stress.The TtMYB1 gene was located in the nucleus.Subsequently, the TtMYB1 overexpression vector was transformed into common wheat.Under NaCl stress, the leaves of the TtMYB1 overexpression lines showed less wilting, and greater root length and seedling height than those of WT plants.In addition, compared to WT plants under salt stress, the overexpression lines had significantly higher proline and soluble sugar content, but lower MDA content.Overall, 51 proteins interacting with TtMYB1 were identified by Y2H.Through PPI analysis, most of the proteins were SANT and Wd repeats region domain-containing proteins, and ribosomal proteins were the main node.Abiotic stress-related terms were enriched in GO analysis.KEGG analysis indicated that "genetic information processing", "signaling and cell precursors", "carbohydrate metabolism", and "environmental information processing" pathways were the most enriched.Thus, the overexpression of the TtMYB1 gene could enhance salt tolerance in wheat and might be a valuable gene for improving crop salt tolerance.

Plant materials
The materials are salt-tolerant octoploid Tritipyrum ("Y1805", AABBDDEE) and salt-sensitive common wheat (AABBDD) "CS", and "1718".Tritipyrum "Y1805" is a stable progeny from a wide cross between Triticum aestivum and Th.elongatum."Y1805" contains A, B, and D chromosomes of wheat, as well as a group of E chromosomes of Th.Elongatum [55]."Y1805" is deposited in Guizhou Subcenter of National Wheat Improvement Center (Guiyang, China).TtMYB1 was transformed into salt-sensitive common wheat "1718" for salt-tolerant identification.

Plant growth conditions and stress treatments
The seeds of Tritipyrum "Y1805" and wheat "CS" were germinated in a growth chamber (relative humidity of 75% and a temperature of 20/15°C, light/dark).The seedlings were sown on a floater board in 1/2 Hoagland's solution with a 16/8 h light/dark cycle, an irradiance of 400 µmol m −2 s −1 , and the same temperature and humidity as in the germination chamber.The culture solution was refreshed every 3 days.At the two-leaf stage (the 14th day after germination), salt stress treatments (1/2 Hoagland's solution added with 250 mM NaCl) were started.The first wheat roots, stems, and leaves of uniform size were selected at 5 h after salt stress according to the preliminary experiments.The materials were recovered in 1/2 Hoagland's solution without NaCl after 24 h of salt stress.The second samplings were performed at 1 h after recovery.Normal (1/2 Hoagland's solution without NaCl) cultured materials were used as the controls.All tissue samples were immediately frozen in liquid nitrogen after sampling and stored at − 80 °C for qPCR analysis and gene cloning.The experiment was conducted with three biological replications, and each replication contained at least 10 seedlings.

Screening of differentially expressed genes (DEGs)
Previous RNA-seq raw reads were deposited into the NCBI SRA database under accession no.PRJNA769794.The DEG screening was based on a method described previously [55].The DEGs potentially regulated by the treatments were identified based on a false discovery rate (FDR) threshold of < 0.01, p < 0.001, and absolute log 2 fold change value (|log 2 FC|) > 1 of the three salt-treated and three salt-free samples using DESeq software [56].The Phyper function in the R package was used for the enrichment analysis of GO categories.

Expression pattern analysis by qPCR
Total RNA from the tissues of roots, stems, and leaves was reverse-transcribed using Power SYBR Green PCR Master Mix (Applied Biosystems, Foster City, CA, USA).Amplification by qPCR was performed on an ABI Ste-pOne Real-Time PCR System.The relative expression levels were calculated using the 2 −ΔΔ Ct method, with three biological replications and three technical replications [57], and 18 S RNA was used as the internal control.

RNA reverse transcription, TtMYB1 amplification and plasmid construction
RNA was reverse-transcribed into cDNA using a Pri-meScript RT kit (Takara, Dalian, China).The full-length coding sequence of TtMYB1 was amplified from the cDNA of "Y1805" using primers containing a BsaI restriction site at the 5′ and 3′ ends of the amplified fragment.The amplification primers are listed in Table S3.The pEGOEPubi-H-TtMYB1-GFP vector was constructed using T4-DNA ligase (Takara) following the manufacturer's protocol.This vector has been modified to contain the GFP gene.The inserted sequence was driven by a corn UBI promoter.

Bioinformatics analysis of the TtMYB1 gene
Multiple alignment of TtMYB1 sequences was performed using DNAMAN with the complete alignment method.Displaying complete base sequence and coloring 100% of homologous bases were selected as the parameters.Online tools Expasy for hydropathy prediction, and Net-Phos 2.0 and CPHmodels 3.2 for phosphorylation site analysis were adopted.The homologous sequences of the MYB protein were retrieved by a BLAST search in the NCBI database (accession numbers in Table S4).A phylogenetic tree was constructed using MEGA 7 (Mega Limited, Auckland, New Zealand) with the maximumlikelihood method and 1000 bootstraps.
Homology modeling of the TtMYB1 protein was performed using MODELLER 9.22 [58].The X-ray crystal structure of a putative MYB protein At2g46140.1 (PDB ID: brp8) was utilized as a template for this procedure.SAVES was used to analyze the predicted model.GROMACS software was used to calculate the RMSD and potential energy value of the model protein [59].Ramachandran plots were analyzed using the Rampage server [60].

Subcellular localization of TtMYB1
The construct containing TtMYB1 was transiently transformed into mesophyll cells prepared from the leaves of 4-week-old tobacco with a polyethylene glycol-mediated protocol.The transformed mesophyll cells were incubated for 72 h at 22 °C in the dark.GFP fluorescence was observed in transformed tobacco mesophyll cells using a confocal laser-scanning microscope (FV1000, Olympus, Tokyo, Japan).

Transformation and detection of TtMYB1
TtMYB1 was transformed into common wheat "1718" according to the wheat coleoptile method [61].For the selection of transformants, seedlings of T 0 transgenic wheat containing the GFP reporter gene were detected using a LUYOR-3415RG hand-held lamp (LUYOR Corporation, Shanghai, China), and planted in a field.Their leaves were sampled at the seedling stage for further PCR identification of transgenic plants.Putative transformants were tested by multiplex PCR amplification of genomic DNA using the specific primers for the UBI promoter and GFP gene, and the primers for the 18 S housekeeping gene (Table S3).PCR products were separated on 1% (w/v) agarose gel.

Phenotype and physiological determination of transgenic wheat
Homozygous T 3 transgenic wheat lines were selected for the assays of growth (root length and seedling height) and physiological analysis.Samples were collected at 0 h (control), 5 h (T1 stage), and 24 h (T2 stage) after salt stress, and at 1 h (R stage) after recovery.The assay kits were applied for measuring proline content (Cas no.: BC0295, Solarbio, Beijing, China), soluble sugar (Cas no.BC0035, Solarbio), and MDA (Cas no.: BC0025, Solarbio) in accordance with the manufacturer's instructions.Three biological replications were performed, and each replication contained at least 10 seedlings for the phenotype and physiological determination in this experiment.

Y2H screen of TtMYB1 interacting proteins
The cDNA library was constructed and identified according to Yang's method [61].The full-length coding sequence of TtMYB1 was inserted into the bait vector pGBKT7 (Takara).The recombinant construct was introduced into the yeast strain Y2HGold using the polyethylene glycol/LiAc method and tested for autoactivation and toxicity.SD-LW and SD-ALWH plates (Coolaber, Beijing, China) were used to screen monoclonal colonies (> 2 mm), and selected colonies were placed in SD-LW liquid medium with shaking during the logarithmic growth phase (29 °C, 200 rpm, 20 h) and then plated on SD-ALWH medium.Positive clones were selected on SD-LW and SD-ALWH (Coolaber) media.The sequencing results of positive clones were analyzed via BLAST.

Switch back prey plasmid and confirmation of positive interactions in yeast
The selected positive clones were extracted using a yeast plasmid extraction kit (Solarbio) and then transformed into E. coli DH5α (Collaborative Innovation Center for the Prevention and Control of Infectious Diseases in the Western Region, Xi'an, China).After culturing, the plasmid was extracted with a plasmid extraction kit (Tiangen, Beijing, China), and the plasmid and pGBKT7-TtMYB1 were co-transformed into yeast Y2HGold cells.The positive cells were screened by coating SD-LW, SD-ALWH, and SD-ALWH/(x-α-gal) auxotrophic plates.GO and KEGG enrichment analyses and PPI analysis were performed for these interacting proteins [62][63][64].

BiFC assays
The BiFC assays were conducted as previously described [65].The full-length cDNAs of TtMYB1 and TtHHO5 were cloned into the vectors of pUC-SPYNE (N terminus of YFP) and pUC-SPYCE (C terminus of YFP) to obtain TtMYB1-nYFP and TtHHO5-cYFP, and then transformed into Agrobacterium (line GV3101).Two vector combinations were co-transformed into 2-4-week-old N. benthamiana leaves.At 72 h after incubation, YFP signals were imaged by confocal laser microscopy (FV1000, Olympus).Nuclei were stained with DAPI (Sigma-Aldrich, St. Louis, USA).Three biological repeats were included for this experiment.This work was funded by the National Natural Science Foundation of China (32160442); the Key Laboratory of Molecular Breeding for Grain and Oil Crops in Guizhou Province (Qiankehezhongyindi (2023) 008); and the Key Laboratory of Functional Agriculture of Guizhou Provincial Higher Education Institutions (Qianjiaoji (2023) 007).

Fig. 1
Fig. 1 Expression levels of MYB in "Y1805" measured by qPCR analysis.A Relative expression levels of the MYB in roots, stems, and leaves under salt stress.B Relative expression levels of MYB in roots under salt stress and in recovery.Bars indicate means with SDs (n = 3).Values with different letters are significantly different at p < 0.05

Fig. 3 Fig. 4 Fig. 5
Fig. 3 Bioinformatics analysis of TtMYB1 protein.A Hydrophilicity.B Protein phosphorylation sites.C Protein domain.D Phylogenetic tree of MYB proteins in various plant species

Fig. 6 Fig. 7
Fig. 6 PCR confirmation of transgenic wheat harboring the TtMYB1 gene.PCR detection of the TtMYB1 gene in the genomic DNA of putative transgenic T 0 wheat leaves.The fragment of the amplified TtMYB1 gene is indicated by a yellow arrow.A white arrow shows the band of the amplified housekeeping 18 S gene.M, 2,000 bp DNA marker; lanes 1, 5, 8, 10, and 12, transgenic plants; lanes 2, 3, 4, 6, 7, 9, and 11, non-transformed plants; P, positive control (TtMYB1 recombinant plasmid); N, negative control (wild-type DNA)

Fig. 8 Fig. 9
Fig. 8 Effect of salt stress and recovery on plant growth.A, B Effects on wheat root length and shoot height.CK, T1, T2, and R represent the control, 5 h after salt stress, 24 h after salt stress, and 1 h after recovery, respectively.The column represents the mean value of SD (n = 3) and values with different letters are significantly different at p < 0.05

Fig. 10
Fig. 10 Identification of non-self-activating TtMYB1 protein and rotational validation of TtMYB1-1 interacting proteins.The SD-LW and SD-ALWH plate had aseptic spots, indicating that the TtMYB1 protein was toxic.SD-LW plates and SD-ALWH plates had plaques, indicating that the TtMYB1 protein had self-activation activity.SD-LW plates had white plaques and SD-ALWH plates had sterile plaques, indicating that the TtMYB1 protein had no self-activating activity.1-51: 51 positive clones were identified.52: Negative control (pGBKT7-laminC).53: Positive control (pGBKT7-p53)

Fig. 11
Fig. 11 TtMYB1 interacting-protein analysis.A Protein-protein interacting analysis.B KEGG pathways of the TtMYB1 potential interacting proteins

Table 2
Main GO terms of TtMYB1 interacting proteins under salt stress